chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14078321	14078322	T	C	67	GENIC	homozygous	142218460
10	14079875	14079876	G	A	50	GENIC	homozygous	142218461
10	14082352	14082353	T	C	41	GENIC	homozygous	142218465
10	14081563	14081564	C	T	48	GENIC	homozygous	142218462
10	14082066	14082067	A	G	53	GENIC	homozygous	142218463
10	14082158	14082159	A	T	62	GENIC	homozygous	142218464
10	14084854	14084855	T	G	20	GENIC	homozygous	142218466
10	14085964	14085965	C	T	45	GENIC	homozygous	142218467
10	14086285	14086286	A	G	51	GENIC	homozygous	142218468
10	14087935	14087936	C	T	51	GENIC	homozygous	142218469
10	14088089	14088090	A	G	60	GENIC	homozygous	142218470
10	14090832	14090833	A	G	53	GENIC	homozygous	142218471
10	14090856	14090857	A	C	51	GENIC	homozygous	142218472
10	14093881	14093882	T	G	54	GENIC	homozygous	142218473
10	14094352	14094353	A	C	64	GENIC	homozygous	142218474
10	14100523	14100524	C	T	60	GENIC	homozygous	142218475
10	14103380	14103382	AA		71	GENIC	homozygous	142196911
10	14082818	14082831	GGTTCGGTCCCCA		39	GENIC	homozygous	142196907
10	14082904	14082908	AACA		43	GENIC	possibly homozygous	142196908
10	14085082	14085083	G		41	GENIC	homozygous	142196909
10	14091852	14091857	TGGTT		48	GENIC	homozygous	142196910
10	14084033	14084034	T	C	60	GENIC	homozygous	138725967
10	14103652	14103653	T	C	66	GENIC	possibly homozygous	142218476
10	14104112	14104113	T	C	46	GENIC	homozygous	142218477
10	14102031	14102032	T		30	GENIC	possibly homozygous	403276920
10	14102031	14102032	T	C	30	GENIC	heterozygous	403276921